Regulatory

Part:BBa_K112701:Design

Designed by: Bing Xia   Group: iGEM08_UC_Berkeley   (2008-10-21)


hns promoter


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Source

Construction of [<Phns>] Basic Part K112701

PCR dv001/dv006 on Phns from E. coli K12 MG1655            (~342 bp, gp = A)
PCR dv005/dv003 on Phns from E. coli K12 MG1655            (225 bp, gp = B)
PCR dv004/dv002 on Phns from E. coli K12 MG1655            (~149 bp, gp = C)
---------------------------------------------------
PCR dv001/dv003 on A+B              (355 bp, gp = D)
---------------------------------------------------
PCR dv001/dv002 on C+D              (697bp, EcoRI/BamHI/DpnI)
Sub into pBca1256                   (EcoRI/BamHI, 2472+697)
Product is pBca1256-K112701
-----------------------------------------------
dv001	Forward Biobricking of [<Phns>]      CgATAgaattcATGagatctGAAATATAGCTGTGCCATCAGCC
dv002	Reverse Biobricking of [<Phns>]      cagtcggatccGCACGAAGAGTACGGATG
dv003  Removing the 2nd EcoRI site in [<Phns>] (R)  GCCAGGAATGTAAGGgATTCAAAATTGTTC
dv004  Removing the 2ND EcoRI site in [<Phns>] (F)  GAACAATTTTGAATcCCTTACATTCCTGGC
dv005  Removing the FIRST EcoRI site in [<Phns>] (F)CGCTTAATAGGGgATTCTCGTAAACAC
dv006  Removing the FIRST EcoRI site in [<Phns>] (R)GTGTTTACGAGAATcCCCTATTAAGCG

References